Status:
NOT_YET_RECRUITING
Hysteroscopic "360°" Surgery for Improvement of Symptoms in Cesarean Scar Defects
Lead Sponsor:
Fu Xing Hospital, Capital Medical University
Conditions:
Cesarean Scar Defect
Eligibility:
FEMALE
18-45 years
Phase:
NA
Brief Summary
Patients with symptomatic Cesarean Scar Defect (CSD) who are expected to undergo hysteroscopic surgery will be randomly divided into the traditional hysteroscopic "channelization" treatment group and ...
Detailed Description
1. Study Design：This is a prospective, randomized controlled trial. 2. Study population 120 patients diagnosed with Cesarean Scar Defect (CSD) will be prospectively recruited. Before the surgery all p...
Eligibility Criteria
Inclusion
- Patients with surgical adaptation: changes in menstruation after cesarean section (prolonged menstrual period)
- No surgical contraindications;
- Age 18-45 years old;
- The thickness of residual muscle layer measured by ultrasound is greater than or equal to 2.5mm;
- Patients with symptoms that have not improved significantly for more than 1 month after oral short-acting contraceptive cycle treatment or who strongly require surgery;
- Understand and agree to the research plan.
Exclusion
- Patients with other diseases that may cause abnormal uterine bleeding (including endometrial polyps, endometrial hyperplasia, submucosal myoma, etc.) indicated by two-dimensional ultrasound
- There are contraindications of surgery: such as severe internal and surgical complications, pregnancy, reproductive tract infection, malignant tumor;
Key Trial Info
Start Date :
May 16 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
November 1 2029
Estimated Enrollment :
88 Patients enrolled
Trial Details
Trial ID
NCT06917014
Start Date
May 16 2025
End Date
November 1 2029
Last Update
May 16 2025
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